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Results: 1-16 |
Results: 16
Evaluation of the role of RANK and OPG genes in Paget's disease of bone
Authors: Wuyts, W Van Wesenbeeck, L Morales-Piga, A Ralston, S Hocking, L Vanhoenacker, F Westhovens, R Verbruggen, L Anderson, D Hughes, A Van Hul, W
Citation: W. Wuyts et al., Evaluation of the role of RANK and OPG genes in Paget's disease of bone, BONE, 28(1), 2001, pp. 104-107
Mechanisms of interleukin 1 beta-induced human airway smooth muscle hyporesponsiveness to histamine - Involvement of p38 MAPK and NF-kappa B
Authors: Pype, JL Xu, HY Schuermans, M Dupont, LJ Wuyts, W Mak, JCW Barnes, PJ Demedts, MG Verleden, GM
Citation: Jl. Pype et al., Mechanisms of interleukin 1 beta-induced human airway smooth muscle hyporesponsiveness to histamine - Involvement of p38 MAPK and NF-kappa B, AM J R CRIT, 163(4), 2001, pp. 1010-1017
Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST)
Authors: Balemans, W Ebeling, M Patel, N Van Hul, E Olson, P Dioszegi, M Lacza, C Wuyts, W Van den Ende, J Willems, P Paes-Alves, AF Hill, S Bueno, M Ramos, FJ Tacconi, P Dikkers, FG Stratakis, C Lindpaintner, K Vickery, B Foernzler, D Van Hul, W
Citation: W. Balemans et al., Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST), HUM MOL GEN, 10(5), 2001, pp. 537-543
Assignment of the mouse Extl1 gene to the distal part of chromosome 4 by in situ hybridization and radiation hybrid mapping
Authors: Mathysen, D Wuyts, W Bossuyt, PJ Wauters, JG Van Hul, W
Citation: D. Mathysen et al., Assignment of the mouse Extl1 gene to the distal part of chromosome 4 by in situ hybridization and radiation hybrid mapping, CYTOG C GEN, 92(1-2), 2001, pp. 162-163
Burning down DEFECT11
Authors: Wuyts, W Van Hul, W Bartsch, O Wilkie, AOM Meinecke, P
Citation: W. Wuyts et al., Burning down DEFECT11, AM J MED G, 100(4), 2001, pp. 331-332
Lack of mutations in the RANK gene in Spanish patients with Paget disease of bone
Authors: Marco-Mingot, M San-Millan, JL Wuyts, W Bachiller-Corral, J Van Hul, W Morales-Piga, AA
Citation: M. Marco-mingot et al., Lack of mutations in the RANK gene in Spanish patients with Paget disease of bone, CLIN GENET, 60(1), 2001, pp. 86-88
A novel deletion mutation of the EXT2 gene in a large Chinese pedigree with hereditary multiple exostosis
Authors: Xia, CY Wang, J Zhang, SZ Van Hul, W Wuyts, W Qiu, WM Wu, H Zhang, G
Citation: Cy. Xia et al., A novel deletion mutation of the EXT2 gene in a large Chinese pedigree with hereditary multiple exostosis, BR J CANC, 85(2), 2001, pp. 176-181
Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35
Authors: Hocking, LJ Herbert, CA Nicholls, RK Williams, F Bennett, ST Cundy, T Nicholson, GC Wuyts, W Van Hul, W Ralston, SH
Citation: Lj. Hocking et al., Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35, AM J HU GEN, 69(5), 2001, pp. 1055-1061
Molecular basis of multiple exostoses: Mutations in the EXT1 and EXT2 genes
Authors: Wuyts, W Van Hul, W
Citation: W. Wuyts et W. Van Hul, Molecular basis of multiple exostoses: Mutations in the EXT1 and EXT2 genes, HUM MUTAT, 15(3), 2000, pp. 220-227
Identification of mutations in the MSX2 homeobox gene in families affectedwith foramina parietalia permagna
Authors: Wuyts, W Reardon, W Preis, S Homfray, T Rasore-Quartino, A Christians, H Willems, PJ Van Hul, W
Citation: W. Wuyts et al., Identification of mutations in the MSX2 homeobox gene in families affectedwith foramina parietalia permagna, HUM MOL GEN, 9(8), 2000, pp. 1251-1255
Organization of the ribosomal operon 16S-23S gene spacer region in representatives of Neisseria gonorrhoeae
Authors: Van Looveren, M Vandamme, P Wuyts, W Ieven, M Goossens, H
Citation: M. Van Looveren et al., Organization of the ribosomal operon 16S-23S gene spacer region in representatives of Neisseria gonorrhoeae, SYST APPL M, 23(1), 2000, pp. 9-14
Characterization and genomic localization of the mouse Extl2 gene
Authors: Wuyts, W Van Hul, W
Citation: W. Wuyts et W. Van Hul, Characterization and genomic localization of the mouse Extl2 gene, CYTOG C GEN, 89(3-4), 2000, pp. 185-188
The ALX4 homeobox gene is mutated in patients with ossification defects ofthe skull (foramina parietalia permagna, OMIM 168500)
Authors: Wuyts, W Cleiren, E Homfray, T Rasore-Quartino, A Vanhoenacker, F Van Hul, W
Citation: W. Wuyts et al., The ALX4 homeobox gene is mutated in patients with ossification defects ofthe skull (foramina parietalia permagna, OMIM 168500), J MED GENET, 37(12), 2000, pp. 916-920
Molecular and clinical examination of an Italian DEFECT 11 family
Authors: Wuyts, W Di Gennaro, G Bianco, F Wauters, J Morocutti, C Pierelli, F Bossuyt, P Van Hul, W Casali, C
Citation: W. Wuyts et al., Molecular and clinical examination of an Italian DEFECT 11 family, EUR J HUM G, 7(5), 1999, pp. 579-584
Refined physical mapping and genomic structure of the EXTL1 gene
Authors: Wuyts, W Spieker, N Van Roy, N De Boulle, K De Paepe, A Willems, PJ Van Hul, W Versteeg, R Speleman, F
Citation: W. Wuyts et al., Refined physical mapping and genomic structure of the EXTL1 gene, CYTOG C GEN, 86(3-4), 1999, pp. 267-270
EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas
Authors: Bovee, JVMG Cleton-Jansen, AM Wuyts, W Caethoven, G Taminiau, AHM Bakker, E Van Hul, W Cornelisse, CJ Hogendoorn, PCW
Citation: Jvmg. Bovee et al., EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas, AM J HU GEN, 65(3), 1999, pp. 689-698
Risultati: 1-16 |